0000000001309942
AUTHOR
Ilaria Giannicchi
Solution and solid-state studies on the halide binding affinity of perfluorophenyl-armed uranyl–salophen receptors enhanced by anion–π Interactions
The enhancement of the binding between halide anions and a Lewis acidic uranyl-salophen receptor has been achieved by the introduction of pendant electron- deficient arene units into the receptor skeleton. The association and the occurrence of the elusive anion-p interaction with halide anions (as tetrabutylammonium salts) have been demonstrated in solution and in the solid state, providing unambiguous evidence on the interplay of the concerted interactions responsible for the anion binding.
CCDC 1427937: Experimental Crystal Structure Determination
Related Article: Luca Leoni, Rakesh Puttreddy, Ondřej Jurček, Andrea Mele, Ilaria Giannicchi, Francesco Yafteh Mihan, Kari Rissanen, Antonella Dalla Cort|2016|Chem.-Eur.J.|22|18714|doi:10.1002/chem.201604313
CCDC 1427936: Experimental Crystal Structure Determination
Related Article: Luca Leoni, Rakesh Puttreddy, Ondřej Jurček, Andrea Mele, Ilaria Giannicchi, Francesco Yafteh Mihan, Kari Rissanen, Antonella Dalla Cort|2016|Chem.-Eur.J.|22|18714|doi:10.1002/chem.201604313